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临床试验/CTRI/2011/10/002046
CTRI/2011/10/002046已完成4 期

DEXMEDETOMIDINE AS AN ADJUNCT TO ANESTHETIC INDUCTION TO ATTENUATE HEMODYNAMIC RESPONSE TO ENDOTRACHEAL INTUBATION IN PATIENTS UNDERGOING SURGICAL PROCEDURES UNDER GENERAL ANESTHESIA

Swai Maan singh Medical College and Attached hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2011年10月10日最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
100
试验地点
1
主要终点
change in systolic, diastolic and mean blood pressure, pulse rate, oxgen saturation compared to baseline at various points before and after intubation compared to baseline

研究概览

简要总结

Conventional laryngoscopy and endotacheal intubation cause significant changes in hemodynamics of patients i.e. increase in heart rate and blood pressure and precipitate arrhythmias which may lead to ischemia and myocardial infarction. In present study dexmedetomidine will be used in combination with fentanyl to attenuate this response.  The aim of study is to study the effect of dexmedetomidine over and above fentanyl in attenuating the hemodynamic response to laryngoscopy and intubation.

In this prospective randomized double blind placebo controlled trial 100 patients will be selected and divided into 2 groups of 50 each. Baseline parameters like body weight , pulse rate and blood pressure will be recorded. Inj.glycopyrolate and inj. fentanyl will be given as premedication. Test drug ( dexmedetomidine/ placebo) will be given by infusion in a double blind fashion. Rate of infusion is adjusted according to body weight. Induction of anesthesia is done with inj. propofol (2mg/kg) and inj. rocuronium (0.8 mg/kg).  laryngoscopy and intubation is done 120 seconds after induction. Blood pressure pulse rate oxgen saturation is recorded at 5, 10, 13 ( just before intubation)   , 14 ( just after intubation), 15, 18, 20 , 25 min after start of infusion. Any intraoperative complication will be noted.Patient will then be extubated at end of procedure after the onset of spontaneous respiration. Statistical anaylsis will be done  using various tests like student-t-test and results and conclusion will be made.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 55.00 Year(s)(—)
性别
All

入选标准

  • 1.Patients with ASA grade 1 and 2 2.Patients of age group 18 to 55 years of either sex undergoing surgery under general anesthesia 3.Patients willing to give written and informed consent.

排除标准

  • 1.Patients refusal 2.Major organ dysfunction 3.Patients on medications like hypnotics, narcotic analgesics, α2 agonists, calcium channel blockers, β blockers 4.Patients with anticipated difficult intubation 5.Patients intubated after more than 1 attempt or more than 20 seconds 6.Patients with impaired LFT/RFT 7.Patients with ASA grade 3, 4, 5 8.Deaf and dumb patients 9.Patients with respiratory and cardiac disease 10.Patients having known allergy to anesthetic agents used in study 11.Psychiatric patients.

结局指标

主要结局

change in systolic, diastolic and mean blood pressure, pulse rate, oxgen saturation compared to baseline at various points before and after intubation compared to baseline

时间窗: 5 , 10 ,13,14(just after intubation),15,18,20,25 min after start of drug infusioon and baseline parameters

次要结局

  • complications like bradycardia , hypotention etc(intraoperative( time period may vary and immediate post operative till 10 min after extubation)

研究者

发起方
Swai Maan singh Medical College and Attached hospital
申办方类型
Government medical college

研究点 (1)

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